Search
for
Sort by
Research 631–660 of 1000+
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Smart Responsive Microneedles for Controlled Drug Delivery
- Electronic States of Epigallocatechin-3-Gallate in Water and in 1,2-dipalmitoyl-sn-glycero-3-phospho-(1′-rac-glycerol) (Sodium Salt) Liposomes
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Regulation of somatic cell reprogramming through inducible mir-302 expression
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Structure and Mechanical Properties of Human Trichocyte Keratin Intermediate Filament Protein
- Leveraging nature’s nanocarriers: Translating insights from extracellular vesicles to biomimetic synthetic vesicles for biomedical applications
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Effect of shampoo, conditioner and permanent waving on the molecular structure of human hair
- Multiplex matrix network analysis of protein complexes in the human TCR signalosome
- Transcriptomic regulation of seasonal coat color change in hares
- Back to the Future: From Appendage Development Toward Future Human Hair Follicle Neogenesis
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair
- The atypical ‘hippocampal’ glutamate receptor coupled to phospholipase D that controls stretch‐sensitivity in primary mechanosensory nerve endings is homomeric purely metabotropic GluK2
- HSP90 Inhibition and Cellular Stress Elicits Phenotypic Plasticity in Hematopoietic Differentiation
- Paxillin regulates androgen receptor expression associated with granulosa cell focal adhesions
- Minoxidil May be a Partial Agonist of Estrogen Receptor Alpha
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Where is the data? Delayed and chronic irAE surveillance and management after cessation of ICIs: expert insights from SITC on survivorship care and the need for long-term data
- Transcriptomic Analysis Provides Molecular Insights into Skin Development in Dezhou Donkey Foals
- Keratin 15 promotes a progenitor cell state in basal keratinocytes of skin epidermis
- Hair regeneration: Mechano-activation and related therapeutic approaches.
- The integrated stress response fine-tunes stem cell fate decisions upon serine deprivation and tissue injury
- Male pattern hair loss: Can developmental origins explain the pattern?